Gillan TL - Search Results

1

Limiting the Niemann-Pick type C critical region to a 1-cM interval.

Gillan TL, Byers DM, Riddell DC, Neumann PE, Greer WL. Gillan TL, et al. Clin Invest Med. 1997 Oct;20(5):339-43. Clin Invest Med. 1997. PMID: 9336659

2

Linkage of Niemann-Pick disease type D to the same region of human chromosome 18 as Niemann-Pick disease type C.

Greer WL, Riddell DC, Byers DM, Welch JP, Girouard GS, Sparrow SM, Gillan TL, Neumann PE. Greer WL, et al. Among authors: gillan tl. Am J Hum Genet. 1997 Jul;61(1):139-42. doi: 10.1086/513899. Am J Hum Genet. 1997. PMID: 9245994 Free PMC article.

3

The Nova Scotia (type D) form of Niemann-Pick disease is caused by a G3097-->T transversion in NPC1.

Greer WL, Riddell DC, Gillan TL, Girouard GS, Sparrow SM, Byers DM, Dobson MJ, Neumann PE. Greer WL, et al. Among authors: gillan tl. Am J Hum Genet. 1998 Jul;63(1):52-4. doi: 10.1086/301931. Am J Hum Genet. 1998. PMID: 9634529 Free PMC article.

4

Linkage disequilibrium mapping of the Nova Scotia variant of Niemann-Pick disease.

Greer WL, Riddell DC, Murty S, Gillan TL, Girouard GS, Sparrow SM, Tatlidil C, Dobson MJ, Neumann PE. Greer WL, et al. Among authors: gillan tl. Clin Genet. 1999 Apr;55(4):248-55. doi: 10.1034/j.1399-0004.1999.550406.x. Clin Genet. 1999. PMID: 10361985

5

A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders.

Innes AM, Boycott KM, Puffenberger EG, Redl D, MacDonald IM, Chudley AE, Beaulieu C, Perrier R, Gillan T, Wade A, Parboosingh JS. Innes AM, et al. Clin Genet. 2010 Nov;78(5):424-31. doi: 10.1111/j.1399-0004.2010.01481.x. Clin Genet. 2010. PMID: 20618352

6

BPES with atypical premature ovarian insufficiency, and evidence of mitotic recombination, in a woman with trisomy X and a translocation t(3;11)(q22.3;q14.1).

Schlade-Bartusiak K, Brown L, Lomax B, Bruyère H, Gillan T, Hamilton S, McGillivray B, Eydoux P. Schlade-Bartusiak K, et al. Am J Med Genet A. 2012 Sep;158A(9):2322-7. doi: 10.1002/ajmg.a.35516. Epub 2012 Aug 6. Am J Med Genet A. 2012. PMID: 22887799

7

Respiratory syncytial virus triggers synthesis of IL-6 in BALB/c mouse alveolar macrophages in the absence of virus replication.

Stadnyk AW, Gillan TL, Anderson R. Stadnyk AW, et al. Among authors: gillan tl. Cell Immunol. 1997 Mar 15;176(2):122-6. doi: 10.1006/cimm.1996.1075. Cell Immunol. 1997. PMID: 9073384

8

Costello syndrome associated with novel germline HRAS mutations: an attenuated phenotype?

Gripp KW, Innes AM, Axelrad ME, Gillan TL, Parboosingh JS, Davies C, Leonard NJ, Lapointe M, Doyle D, Catalano S, Nicholson L, Stabley DL, Sol-Church K. Gripp KW, et al. Among authors: gillan tl. Am J Med Genet A. 2008 Mar 15;146A(6):683-90. doi: 10.1002/ajmg.a.32227. Am J Med Genet A. 2008. PMID: 18247425

9

Cytogenetic and molecular characterization of a de-novo cryptic deletion of 7p21 associated with an apparently balanced translocation and complex craniosynostosis.

Shetty S, Boycott KM, Gillan TL, Bowser K, Parboosingh JS, McInnes B, Chernos JE, Bernier FP. Shetty S, et al. Among authors: gillan tl. Clin Dysmorphol. 2007 Oct;16(4):253-6. doi: 10.1097/MCD.0b013e3281e668eb. Clin Dysmorphol. 2007. PMID: 17786117

10

An undiagnosed cytogenetic abnormality results in the misidentification of a Duchenne muscular dystrophy carrier.

Gillan TL, Davies C, Innes AM, Howard J, Graham L, Chernos J, Bridge PJ, Parboosingh JS. Gillan TL, et al. Am J Med Genet A. 2008 Apr 15;146A(8):1067-71. doi: 10.1002/ajmg.a.32231. Am J Med Genet A. 2008. PMID: 18348271 No abstract available.

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